Machine-learning guided Venom Induced Dermonecrosis Analysis tooL: VIDAL

William Laprade, Keirah Bartlett, Charlotte R. Christensen, Taline Kazandjian, Rohit Patel, Edouard Crittenden, Charlotte Dawson, Marjan Mansourvar, Darian S. Wolff, Thomas Fryer, Andreas H. Laustsen, Nick Casewell, José María Gutiérrez, Steven R. Hall, Timothy P. Jenkins

Research output: Contribution to journalArticlepeer-review

5 Citations (Scopus)

Abstract

Snakebite envenoming is a global public health issue that causes significant morbidity and mortality, particularly in low-income regions of the world. The clinical manifestations of envenomings vary depending on the snake's venom, with paralysis, haemorrhage, and necrosis being the most common and medically relevant effects. To assess the efficacy of antivenoms against dermonecrosis, a preclinical testing approach involves in vivo mouse models that mimic local tissue effects of cytotoxic snakebites in humans. However, current methods for assessing necrosis severity are time-consuming and susceptible to human error. To address this, we present the Venom Induced Dermonecrosis Analysis tooL (VIDAL), a machine-learning-guided image-based solution that can automatically identify dermonecrotic lesions in mice, adjust for lighting biases, scale the image, extract lesion area and discolouration, and calculate the severity of dermonecrosis. We also introduce a new unit, the dermonecrotic unit (DnU), to better capture the complexity of dermonecrosis severity. Our tool is comparable to the performance of state-of-the-art histopathological analysis, making it an accessible, accurate, and reproducible method for assessing dermonecrosis in mice. Given the urgent need to address the neglected tropical disease that is snakebite, high-throughput technologies such as VIDAL are crucial in developing and validating new and existing therapeutics for this debilitating disease.

Original languageEnglish
Article number21662
Pages (from-to)e21662
JournalScientific Reports
Volume13
Issue number1
Early online date8 Dec 2023
DOIs
Publication statusPublished - 8 Dec 2023

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